| 产品描述: | Pibrentasvir (ABT-530) 是一种新型的泛基因型丙型肝炎病毒 hepatitis C virus (HCV) NS5A 抑制剂,其针对包含基因型1至6的NS5A的HCV复制子的EC50值为1.4 pM至5.0 pM |
| 靶点: |
GT5a(Cell-free assay):1.4 pM(EC50); GT1a H77(Cell-free assay):1.8 pM(EC50); GT2b(Cell-free assay):1.9 pM(EC50); GT4a(Cell-free assay):1.9 pM(EC50); GT3a(Cell-free assay):2.1 pM(EC50);GT2ab(Cell-free assay):2.3 pM;GT6a(Cell-free assay):2.8 pM;GT1b Con1(Cell-free assay):4.3 pM;GT2a JFH-1(Cell-free assay):5.0 pM;HCVProtease |
| 细胞实验: |
Cell lines: Huh-7 human hepatoma cell line, CEM-SS cells Concentrations: -- Incubation Time: 6 days Method: Antiviral activity assays for HIV-1 and HBV are performed at Southern Research Institute. Pibrentasvir is tested in an HIV-1 antiviral cytoprotection assay using CEM-SS cells and the IIIB strain of HIV-1. Briefly, virus and cells are mixed in the presence of pibrentasvir or zidovudine (AZT; positive control) and incubated for 6 days. The titers of the virus are determined beforehand such that the virus-infected control wells exhibited approximately 85% to 95% loss of cell viability due to virus replication. Therefore, antiviral effect or cytoprotection is observed when a compound prevented virus replication. Six days after infection, 20 to 25 μl of MTS reagent is added per well, and the microtiter plates are then incubated for 4 to 6 h to assess cell viability. Plates are read spectrophotometrically at 490/650 nm with a Molecular Devices Vmax or SpectraMax Plus plate reader. |
| 参考文献: |
1. Teresa I Ng, et al. Antimicrob Agents Chemother. 2017 Apr 24;61(5):e02558-16. |
| 溶解性: |
Soluble in DMSO、Ethanol |
| 保存条件: |
-20°C |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
0.898 ml |
4.492 ml |
8.983 ml |
| 5 mM |
0.18 ml |
0.898 ml |
1.797 ml |
| 10 mM |
0.09 ml |
0.449 ml |
0.898 ml |
| 50 mM |
0.018 ml |
0.09 ml |
0.18 ml |
|
| 注意: |
部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。 |